Bayesian designs for phase I-II clinical trials / Ying Yuan, The University of Texas, MD Anderson Cancer Center, Houston, Texas, USA; Hoang Q. Nguyen,The University of Texas, MD Anderson Cancer Center, Houston, Texas, USA; Peter F. Thall The University of Texas, MD Anderson Cancer Center, Houston, Texas, USA.
By: Yuan, Ying (Professor of biostatistics)
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Contributor(s): Nguyen, Hoang Q
| Thall, Peter F
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Item type | Current location | Collection | Call number | Status | Date due | Barcode | Item holds |
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RGU Central Library Reference | Reference | 615.50724 YUA-B (Browse shelf) | Not for loan | 77875 |
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615.3252 ITO-T Taxus | 615.403 OFF-E Encyclopedia of molecular pharmacology | 615.403 OFF-E Encyclopedia of molecular pharmacology | 615.50724 YUA-B Bayesian designs for phase I-II clinical trials / | 615.580724 HOU-D Dynamic prediction in clinical survival analysis: | 615.6 LOR-S Smart materials for drug delivery: | 615.6 LOR-S Smart materials for drug delivery: |
Includes bibliographical references (pages 283-300) and index.
Why conduct phase I-II trials? -- The phase I-II paradigm -- Establishing priors -- Efficacy-toxicity trade-off-based designs -- Designs with late-onset outcomes -- Utility-based designs -- Personalized dose finding -- Combination trials -- Optimizing molecularly targeted agents -- Optimizing doses in two cycles -- Optimizing dose and schedule -- Dealing with dropouts -- Optimizing intra-arterial tPA -- Optimizing sedative dose in preterm infants.
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